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CO Sensing Performance of a Micro Thermoelectric Gas Sensor with AuPtPd/SnO2 Catalyst and Effects of a Double Catalyst Structure with Pt/α-Al2O3

机译:AuPtPd / SnO2催化剂的微热电气体传感器的CO传感性能以及Pt /α-Al2O3的双重催化剂结构的影响

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摘要

The CO sensing properties of a micro thermoelectric gas sensor (micro-TGS) with a double AuPtPd/SnO2 and Pt/α-Al2O3 catalyst were investigated. While several nanometer sized Pt and Pd particles were uniformly dispersed on SnO2, the Au particles were aggregated as particles measuring >10 nm in diameter. In situ diffuse reflectance Fourier transform Infrared spectroscopy (DRIFT) analysis of the catalyst showed a CO adsorption peak on Pt and Pd, but no clear peak corresponding to the interaction between CO and Au was detected. Up to 200 °C, CO combustion was more temperature dependent than that of H2, while H2 combustion was activated by repeated exposure to H2 gas during the periodic gas test. Selective CO sensing of the micro-TGS against H2 was attempted using a double catalyst structure with 0.3–30 wt% Pt/α-Al2O3 as a counterpart combustion catalyst. The sensor output of the micro-TGS decreased with increasing Pt content in the Pt/α-Al2O3 catalyst, by cancelling out the combustion heat from the AuPtPd/SnO2 catalyst. In addition, the AuPtPd/SnO2 and 0.3 wt% Pt/α-Al2O3 double catalyst sensor showed good and selective CO detection. We therefore demonstrated that our micro-TGS with double catalyst structure is useful for controlling the gas selectivity of CO against H2.
机译:研究了具有双重AuPtPd / SnO2和Pt /α-Al2O3催化剂的微热电气体传感器(micro-TGS)的CO感测特性。当数个纳米级的Pt和Pd颗粒均匀地分散在SnO2上时,Au颗粒聚集为直径大于10 nm的颗粒。催化剂的原位漫反射傅里叶变换红外光谱(DRIFT)分析显示Pt和Pd上的CO吸附峰,但未检测到与CO和Au相互作用相对应的清晰峰。在高达200°C的温度下,CO燃烧比H2对温度的依赖性更大,而在定期的气体测试过程中,通过反复暴露于H2气体激活了H2燃烧。尝试使用具有0.3–30 wt%的Pt /α-Al2O3作为辅助燃烧催化剂的双重催化剂结构,对微型TGS对H2进行选择性CO感测。通过抵消AuPtPd / SnO2催化剂的燃烧热,微型TGS的传感器输出随Pt /α-Al2O3催化剂中Pt含量的增加而降低。此外,AuPtPd / SnO2和0.3 wt%Pt /α-Al2O3双催化剂传感器显示出良好的选择性CO检测。因此,我们证明了具有双重催化剂结构的微型TGS可用于控制CO对H 2 的气体选择性。

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